Canonical Allele Identifier: PA340065
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Arg246Trp
CA340064
NM_000348.4:c.736C>T